LRRIQ1

leucine rich repeats and IQ motif containing 1

Summary

Predicted to be involved in regulation of signal transduction. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants113 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2499037723	12:85,431,968	A/T	—	uncertain significance
rs766219757	12:85,431,989	T/C	—	uncertain significance
rs200816060	12:85,431,995	C/T	—	uncertain significance
rs374855317	12:85,438,580	T/C	—	uncertain significance
rs774053980	12:85,439,810	A/G	—	uncertain significance
rs781016761	12:85,439,843	G/T	—	uncertain significance
rs149503974	12:85,439,864	G/A	—	uncertain significance
rs140252116	12:85,439,865	T/C	—	uncertain significance
rs1255765926	12:85,441,077	G/C	—	uncertain significance
rs766173852	12:85,441,135	C/G	—	uncertain significance
rs761527744	12:85,441,151	A/C	—	uncertain significance
rs142687579	12:85,441,217	T/C	—	uncertain significance
rs774218237	12:85,446,006	A/G	—	uncertain significance
rs61740062	12:85,446,018	A/C	—	uncertain significance
rs200254104	12:85,449,355	G/A	—	uncertain significance
rs112921634	12:85,449,358	G/A	—	uncertain significance
rs750770453	12:85,449,404	C/A	—	uncertain significance
rs781405194	12:85,449,457	G/A	—	uncertain significance
rs201694390	12:85,449,499	C/G	—	uncertain significance
rs772693447	12:85,449,529	G/A	—	uncertain significance
rs1161556230	12:85,449,536	A/T	—	uncertain significance
rs200640188	12:85,449,557	G/A	—	uncertain significance
rs756097902	12:85,449,578	G/T	—	uncertain significance
rs775801562	12:85,449,674	A/G	—	uncertain significance
rs148534712	12:85,449,689	A/C	—	uncertain significance
rs754722038	12:85,449,711	C/A	—	uncertain significance
rs539161034	12:85,449,723	A/G	—	uncertain significance
rs755969062	12:85,449,812	A/G	—	uncertain significance
rs2499230720	12:85,449,827	A/C	—	uncertain significance
rs1239650105	12:85,449,943	A/G	—	uncertain significance
rs1301221845	12:85,449,968	A/G	—	uncertain significance
rs140993343	12:85,449,980	C/T	—	uncertain significance
rs2499239034	12:85,450,163	A/C	—	uncertain significance
rs762937434	12:85,450,262	G/A	—	likely benign
rs200192265	12:85,450,291	A/G	—	uncertain significance
rs758484541	12:85,450,303	A/C	—	uncertain significance
rs145492155	12:85,450,365	A/T	—	uncertain significance
rs200559703	12:85,450,407	A/T	—	uncertain significance
rs1303911195	12:85,450,408	T/A	—	uncertain significance
rs1331226552	12:85,450,414	T/C	—	likely benign
rs371965033	12:85,450,429	A/G	—	uncertain significance
rs762250297	12:85,450,501	G/A	—	uncertain significance
rs2499249156	12:85,450,528	A/G	—	uncertain significance
rs1881141451	12:85,450,549	A/G	—	uncertain significance
rs1203544550	12:85,450,574	A/G	—	uncertain significance
rs2499250711	12:85,450,595	A/G	—	uncertain significance
rs758123514	12:85,450,679	C/G	—	uncertain significance
rs775456418	12:85,450,756	G/A	—	uncertain significance
rs1351643627	12:85,450,797	A/C	—	uncertain significance
rs544935621	12:85,450,903	A/T	—	uncertain significance
rs1328845173	12:85,459,053	C/A	—	uncertain significance
rs769803503	12:85,459,087	A/C	—	likely benign
rs2499346217	12:85,459,157	A/T	—	uncertain significance
rs1332312242	12:85,459,184	G/A	—	uncertain significance
rs201707498	12:85,460,533	A/G	—	likely benign
rs147534931	12:85,460,542	C/A	—	uncertain significance
rs564746060	12:85,460,611	A/G	—	uncertain significance
rs765843926	12:85,466,690	T/G	—	uncertain significance
rs773796685	12:85,466,691	C/T	—	uncertain significance
rs760765297	12:85,466,753	A/G	—	uncertain significance
rs200596040	12:85,492,216	C/A	—	uncertain significance
rs202069982	12:85,492,287	G/C	—	uncertain significance
rs1438535984	12:85,492,718	C/T	—	uncertain significance
rs768644704	12:85,492,759	A/C	—	likely benign
rs748752901	12:85,497,813	G/A	—	uncertain significance
rs761108643	12:85,497,840	C/G	—	uncertain significance
rs139188004	12:85,497,847	G/T	—	uncertain significance
rs147080103	12:85,515,500	G/A	—	uncertain significance
rs1393488672	12:85,515,540	C/T	—	uncertain significance
rs766184197	12:85,515,641	A/G	—	uncertain significance
rs1461413215	12:85,515,643	A/G	—	uncertain significance
rs374288998	12:85,517,855	T/C	—	uncertain significance
rs1472234240	12:85,517,900	T/A	—	uncertain significance
rs770626027	12:85,517,909	C/G	—	uncertain significance
rs200154815	12:85,517,936	G/A	—	uncertain significance
rs367637593	12:85,517,943	G/T	—	uncertain significance
rs775555011	12:85,518,003	C/A	—	uncertain significance
rs1252810004	12:85,518,007	C/A	—	uncertain significance
rs377176302	12:85,518,105	C/T	—	uncertain significance
rs377703986	12:85,518,195	G/A	—	uncertain significance
rs1482214955	12:85,518,204	G/A	—	uncertain significance
rs2499750850	12:85,518,207	G/C	—	uncertain significance
rs760879565	12:85,518,236	G/C	—	uncertain significance
rs141671586	12:85,518,255	C/A	—	uncertain significance
rs748072772	12:85,521,614	G/A	—	uncertain significance
rs549621904	12:85,521,657	G/A	—	uncertain significance
rs749863431	12:85,521,696	C/T	—	uncertain significance
rs757973024	12:85,521,777	G/A	—	likely benign
rs1173969835	12:85,531,641	G/C	—	uncertain significance
rs763842615	12:85,531,682	A/G	—	uncertain significance
rs915880508	12:85,531,715	G/A	—	uncertain significance
rs2499907714	12:85,546,873	T/G	—	uncertain significance
rs1462325478	12:85,547,452	A/G	—	likely benign
rs2499911518	12:85,547,472	G/C	—	uncertain significance
rs746399504	12:85,547,515	A/G	—	uncertain significance
rs775724645	12:85,547,524	T/C	—	uncertain significance
rs778415975	12:85,547,836	C/G	—	uncertain significance
rs758802431	12:85,547,849	C/T	—	uncertain significance
rs761433062	12:85,554,425	T/G	—	uncertain significance
rs766067329	12:85,554,448	A/T	—	uncertain significance

Showing 100 of 113 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.